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Year Number of Results
2002 1
2003 2
2004 1
2005 1
2006 3
2007 4
2008 1
2009 4
2010 3
2011 4
2012 1
2013 3
2014 3
2015 4
2016 6
2017 8
2018 11
2019 8
2020 8
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2022 7
2023 6
2024 2

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Page 1
International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up.
Altassan R, Péanne R, Jaeken J, Barone R, Bidet M, Borgel D, Brasil S, Cassiman D, Cechova A, Coman D, Corral J, Correia J, de la Morena-Barrio ME, de Lonlay P, Dos Reis V, Ferreira CR, Fiumara A, Francisco R, Freeze H, Funke S, Gardeitchik T, Gert M, Girad M, Giros M, Grünewald S, Hernández-Caselles T, Honzik T, Hutter M, Krasnewich D, Lam C, Lee J, Lefeber D, Marques-de-Silva D, Martinez AF, Moravej H, Õunap K, Pascoal C, Pascreau T, Patterson M, Quelhas D, Raymond K, Sarkhail P, Schiff M, Seroczyńska M, Serrano M, Seta N, Sykut-Cegielska J, Thiel C, Tort F, Vals MA, Videira P, Witters P, Zeevaert R, Morava E. Altassan R, et al. Among authors: borgel d. J Inherit Metab Dis. 2019 Jan;42(1):5-28. doi: 10.1002/jimd.12024. J Inherit Metab Dis. 2019. PMID: 30740725
Pathogenesis of meningococcal purpura fulminans.
Lécuyer H, Borgel D, Nassif X, Coureuil M. Lécuyer H, et al. Among authors: borgel d. Pathog Dis. 2017 Apr 1;75(3). doi: 10.1093/femspd/ftx027. Pathog Dis. 2017. PMID: 28334263 Review.
Trends in the development of oral anticoagulants.
Ralay-Ranaivo B, Borgel D, Couvreur P, Gref R. Ralay-Ranaivo B, et al. Among authors: borgel d. Ther Deliv. 2015;6(6):685-703. doi: 10.4155/tde.15.22. Ther Deliv. 2015. PMID: 26149785 Review.
MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation.
Kauskot A, Mallebranche C, Bruneel A, Fenaille F, Solarz J, Viellard T, Feng M, Repérant C, Bordet JC, Cholet S, Denis CV, McCluskey G, Latour S, Martin E, Pellier I, Lasne D, Borgel D, Kracker S, Ziegler A, Tuffigo M, Fournier B, Miot C, Adam F. Kauskot A, et al. Among authors: borgel d. J Thromb Haemost. 2023 Nov;21(11):3268-3278. doi: 10.1016/j.jtha.2023.05.007. Epub 2023 May 18. J Thromb Haemost. 2023. PMID: 37207862
Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylation.
Čechová A, Altassan R, Borgel D, Bruneel A, Correia J, Girard M, Harroche A, Kiec-Wilk B, Mohnike K, Pascreau T, Pawliński Ł, Radenkovic S, Vuillaumier-Barrot S, Aldamiz-Echevarria L, Couce ML, Martins EG, Quelhas D, Morava E, de Lonlay P, Witters P, Honzík T. Čechová A, et al. Among authors: borgel d. J Inherit Metab Dis. 2020 Jul;43(4):671-693. doi: 10.1002/jimd.12241. Epub 2020 Apr 21. J Inherit Metab Dis. 2020. PMID: 32266963 Free PMC article. Review.
How can the design of therapeutic SERPINs be improved?
Bianchini E, Auditeau C, Borgel D. Bianchini E, et al. Among authors: borgel d. J Thromb Haemost. 2022 May;20(5):1037-1039. doi: 10.1111/jth.15667. Epub 2022 Feb 17. J Thromb Haemost. 2022. PMID: 35174614 Free article. No abstract available.
Hemostatic defects in congenital disorders of glycosylation.
Pascreau T, Auditeau C, Borgel D. Pascreau T, et al. Among authors: borgel d. Res Pract Thromb Haemost. 2023 Mar 30;7(3):100142. doi: 10.1016/j.rpth.2023.100142. eCollection 2023 Mar. Res Pract Thromb Haemost. 2023. PMID: 37193126 Free PMC article.
[Coagulation factor mutations and thrombosis].
Aiach M, Alhenc-Gelas M, Borgel D, Emmerich J, Gandrille S, Picard V. Aiach M, et al. Among authors: borgel d. Med Sci (Paris). 2006 Nov;22(11):985-9. doi: 10.1051/medsci/20062211985. Med Sci (Paris). 2006. PMID: 17101102 Free article. Review. French.
87 results